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Items: 1 to 50 of 163

1.

[A Case of Gastric Cancer with Necrotic Lymph Node Perforation in the Stomach during Chemotherapy].

Suito H, Shinoto K, Okazaki Y, Matsuo K, Hirano A, Sato K, Hanaoka T, Aida N, Ikeda Y, Murakami T.

Gan To Kagaku Ryoho. 2019 Sep;46(9):1437-1439. Japanese.

PMID:
31530785
2.

The Effects of Using Pancreases Obtained from Brain-Dead Donors for Clinical Islet Transplantation in Japan.

Ito T, Kenmochi T, Kurihara K, Kawai A, Aida N, Akashi Y, Kato S.

J Clin Med. 2019 Sep 10;8(9). pii: E1430. doi: 10.3390/jcm8091430.

3.

The Outcomes of Pancreatic Transplantation from Pediatric Donors-A Single Institution Experience.

Ito T, Kenmochi T, Aida N, Kurihara K, Kawai A, Suzuki A, Shibata M, Hiratsuka I, Hasegawa M.

J Clin Med. 2019 Sep 4;8(9). pii: E1386. doi: 10.3390/jcm8091386.

4.

Lack of association of ovariectomy-induced obesity with overeating and the reduction of physical activities.

Nishio E, Hayashi T, Nakatani M, Aida N, Suda R, Fujii T, Wakatsuki T, Honda S, Harada N, Shimono Y.

Biochem Biophys Rep. 2019 Aug 8;20:100671. doi: 10.1016/j.bbrep.2019.100671. eCollection 2019 Dec.

5.

A Case of Epstein-Barr Virus-Associated Leiomyosarcoma Concurrently With Posttransplant Lymphoproliferative Disorders After Renal Transplantation.

Aida N, Ito T, Maruyama M, Saigo K, Akutsu N, Aoyama H, Kitamura H, Kenmochi T.

Clin Med Insights Case Rep. 2019 Jul 31;12:1179547619867330. doi: 10.1177/1179547619867330. eCollection 2019.

6.

Effectiveness of Preceding Solo Kidney Transplantation for Type 1 Diabetes With End-Stage Renal Failure.

Ito T, Kenmochi T, Aida N, Kurihara K, Kawai A, Ito T.

Transplant Proc. 2018 Dec;50(10):3249-3254. doi: 10.1016/j.transproceed.2018.06.014. Epub 2018 Jun 22.

PMID:
30577193
7.

Imaging of Cystic Lung Lesions in Infants Using Pointwise Encoding Time Reduction with Radial Acquisition (PETRA).

Nozawa K, Niwa T, Aida N.

Magn Reson Med Sci. 2019 Oct 15;18(4):299-300. doi: 10.2463/mrms.bc.2018-0080. Epub 2018 Dec 3. No abstract available.

8.

Aggregate formation analysis of GFAPR416W found in one case of Alexander disease.

Tulyeu J, Tamaura M, Jimbo E, Shimbo H, Takano K, Iai M, Yamashita S, Goto T, Aida N, Tokuhiro E, Yamagata T, Osaka H.

Brain Dev. 2019 Feb;41(2):195-200. doi: 10.1016/j.braindev.2018.08.009. Epub 2018 Sep 10.

PMID:
30213442
9.

"Thumb's off" for acrometastasis of renal cell carcinoma: Is there a role for acrometastasectomy in the era of targeted therapy?

Lechmiannandan S, Aida N, Paul AG, Thevarajah S.

Asian J Urol. 2018 Jul;5(3):199-201. doi: 10.1016/j.ajur.2017.07.003. Epub 2017 Oct 16. No abstract available.

10.

Changes in Brain Metabolite Concentrations after Neonatal Hypoxic-ischemic Encephalopathy.

Shibasaki J, Aida N, Morisaki N, Tomiyasu M, Nishi Y, Toyoshima K.

Radiology. 2018 Sep;288(3):840-848. doi: 10.1148/radiol.2018172083. Epub 2018 Jun 12.

PMID:
29893645
11.

MR imaging findings in some rare neurological complications of paediatric cancer.

Okabe T, Nozaki T, Aida N, Starkey J, Enokizono M, Niwa T, Handa A, Numaguchi Y, Kurihara Y.

Insights Imaging. 2018 Jun;9(3):313-324. doi: 10.1007/s13244-018-0628-z. Epub 2018 May 15. Review.

12.

Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly.

Sato Y, Shibasaki J, Aida N, Hiiragi K, Kimura Y, Akahira-Azuma M, Enomoto Y, Tsurusaki Y, Kurosawa K.

Hum Genome Var. 2018 Apr 24;5:4. doi: 10.1038/s41439-018-0005-y. eCollection 2018.

13.

Prediction of Insulin Secretion Ability With Microcirculation Evaluated by Contrast-enhanced Ultrasonography in Pancreas Transplantation.

Aida N, Kenmochi T, Ito T, Nishikawa T, Hiratsuka I, Shibata M, Suzuki A, Hasegawa M, Kawai A, Kusaka M, Hoshinaga K, Matsubara H.

Pancreas. 2018 May/Jun;47(5):617-624. doi: 10.1097/MPA.0000000000001051.

PMID:
29683975
14.

Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound.

Ohwaki A, Nishizawa H, Aida N, Kato T, Kambayashi A, Miyazaki J, Ito M, Urano M, Kiriyama Y, Kuroda M, Nakayama M, Sonta SI, Suzumori K, Sekiya T, Kurahashi H, Fujii T.

J Obstet Gynaecol. 2018 Oct;38(7):1023-1025. doi: 10.1080/01443615.2017.1401598. Epub 2018 Mar 9. No abstract available.

PMID:
29523025
15.

Serial Magnetic Resonance Imaging and 1H-Magnetic Resonance Spectroscopy in GABA Transaminase Deficiency: A Case Report.

Ichikawa K, Tsuji M, Tsuyusaki Y, Tomiyasu M, Aida N, Goto T.

JIMD Rep. 2019;43:7-12. doi: 10.1007/8904_2018_95. Epub 2018 Feb 25.

16.

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis.

Enomoto Y, Tsurusaki Y, Harada N, Aida N, Kurosawa K.

Congenit Anom (Kyoto). 2018 Jul;58(4):145-146. doi: 10.1111/cga.12258. Epub 2017 Nov 16. No abstract available.

PMID:
28990699
17.

Response of porcine epithelial rests of Malassez to stimulation by interleukin-6.

Sako R, Kobayashi F, Aida N, Furusawa M, Muramatsu T.

Int Endod J. 2018 Apr;51(4):431-437. doi: 10.1111/iej.12862. Epub 2017 Oct 10.

PMID:
28898425
18.

Renal Autotransplantation and Extracorporeal Nephron-Sparing Surgery for De Novo Renal Cell Carcinoma in a Kidney Allograft.

Ono S, Kenmochi T, Ito T, Aida N, Otsuki K, Akutsu N, Maruyama M, Kusaka M, Shiroki R, Hoshinaga K.

Transplant Direct. 2017 Jul 24;3(8):e122. doi: 10.1097/TXD.0000000000000714. eCollection 2017 Aug.

19.

Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome.

Shimbo H, Yokoi T, Aida N, Mizuno S, Suzumura H, Nagai J, Ida K, Enomoto Y, Hatano C, Kurosawa K.

Mol Genet Genomic Med. 2017 May 22;5(4):429-437. doi: 10.1002/mgg3.289. eCollection 2017 Jul.

20.

A novel UBE2A mutation causes X-linked intellectual disability type Nascimento.

Tsurusaki Y, Ohashi I, Enomoto Y, Naruto T, Mitsui J, Aida N, Kurosawa K.

Hum Genome Var. 2017 Jun 8;4:17019. doi: 10.1038/hgv.2017.19. eCollection 2017.

21.

Usefulness of Interprofessional Education (Tsurumai-Meijo IPE) in Program Collaborating with Simulated Patients.

Goto A, Hanya M, Yoshimi A, Uchida M, Takeuchi S, Aida N, Suematsu M, Abe K, Yasui H, Kamei H, Noda Y.

Yakugaku Zasshi. 2017;137(6):733-744. doi: 10.1248/yakushi.16-00215. Japanese.

22.

Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia.

Enokizono M, Aida N, Niwa T, Osaka H, Naruto T, Kurosawa K, Ohba C, Suzuki T, Saitsu H, Goto T, Matsumoto N.

J Neurol Sci. 2017 May 15;376:7-12. doi: 10.1016/j.jns.2017.02.065. Epub 2017 Mar 1.

PMID:
28431631
23.

A small pons as a characteristic finding in Down syndrome: A quantitative MRI study.

Fujii Y, Aida N, Niwa T, Enokizono M, Nozawa K, Inoue T.

Brain Dev. 2017 Apr;39(4):298-305. doi: 10.1016/j.braindev.2016.10.016. Epub 2016 Nov 16.

PMID:
27865668
24.

In vivo estimation of gamma-aminobutyric acid levels in the neonatal brain.

Tomiyasu M, Aida N, Shibasaki J, Umeda M, Murata K, Heberlein K, Brown MA, Shimizu E, Tsuji H, Obata T.

NMR Biomed. 2017 Jan;30(1). doi: 10.1002/nbm.3666. Epub 2016 Nov 11.

25.

Visualization of the airway in infants with MRI using pointwise encoding time reduction with radial acquisition (PETRA).

Niwa T, Nozawa K, Aida N.

J Magn Reson Imaging. 2017 Mar;45(3):839-844. doi: 10.1002/jmri.25420. Epub 2016 Aug 4.

PMID:
27490158
26.

Normal lactate concentration range in the neonatal brain.

Tomiyasu M, Aida N, Shibasaki J, Tachibana Y, Endo M, Nozawa K, Shimizu E, Tsuji H, Obata T.

Magn Reson Imaging. 2016 Nov;34(9):1269-1273. doi: 10.1016/j.mri.2016.07.006. Epub 2016 Jul 25.

PMID:
27466138
27.

Influence of ADORA2A gene polymorphism on leukoencephalopathy risk in MTX-treated pediatric patients affected by hematological malignancies.

Tsujimoto S, Yanagimachi M, Tanoshima R, Urayama KY, Tanaka F, Aida N, Goto H, Ito S.

Pediatr Blood Cancer. 2016 Nov;63(11):1983-9. doi: 10.1002/pbc.26090. Epub 2016 Jul 11.

PMID:
27399166
28.

Quiet T1-Weighted Pointwise Encoding Time Reduction with Radial Acquisition for Assessing Myelination in the Pediatric Brain.

Aida N, Niwa T, Fujii Y, Nozawa K, Enokizono M, Murata K, Obata T.

AJNR Am J Neuroradiol. 2016 Aug;37(8):1528-34. doi: 10.3174/ajnr.A4747. Epub 2016 Apr 7.

29.

The reliability and validity of the Japanese version of the Temperament and Personality Questionnaire for patients with non-melancholic depression.

Kudo Y, Nakagawa A, Tamura N, Kato N, Williams A, Aida N, Mimura M.

J Affect Disord. 2016 Jul 1;198:237-41. doi: 10.1016/j.jad.2016.03.046. Epub 2016 Mar 26.

30.

WDR45 mutations in three male patients with West syndrome.

Nakashima M, Takano K, Tsuyusaki Y, Yoshitomi S, Shimono M, Aoki Y, Kato M, Aida N, Mizuguchi T, Miyatake S, Miyake N, Osaka H, Saitsu H, Matsumoto N.

J Hum Genet. 2016 Jul;61(7):653-61. doi: 10.1038/jhg.2016.27. Epub 2016 Mar 31. Review.

PMID:
27030146
31.

Single institution outcomes in the first 3 years of pancreas transplantation from brain dead donors.

Ito T, Kenmochi T, Ono S, Oshima M, Aida N, Suzuki A, Hasegawa M, Kusaka M, Hoshinaga K.

J Hepatobiliary Pancreat Sci. 2016 May;23(5):270-5. doi: 10.1002/jhbp.339. Epub 2016 Mar 30.

PMID:
26945910
32.

Interhemispheric Lipoma, Callosal Anomaly, and Malformations of Cortical Development: A Case Series.

Niwa T, de Vries LS, Manten GT, Lequin M, Cuppen I, Shibasaki J, Aida N.

Neuropediatrics. 2016 Apr;47(2):115-8. doi: 10.1055/s-0035-1570752. Epub 2016 Jan 25.

PMID:
26808679
33.

Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia Pigmenti.

Tomotaki S, Shibasaki J, Yunoki Y, Kishigami M, Imagawa T, Aida N, Toyoshima K, Itani Y.

Pediatr Neurol. 2016 Mar;56:55-58. doi: 10.1016/j.pediatrneurol.2015.12.002. Epub 2015 Dec 18.

PMID:
26777982
34.

Elevation of neuron specific enolase and brain iron deposition on susceptibility-weighted imaging as diagnostic clues for beta-propeller protein-associated neurodegeneration in early childhood: Additional case report and review of the literature.

Takano K, Shiba N, Wakui K, Yamaguchi T, Aida N, Inaba Y, Fukushima Y, Kosho T.

Am J Med Genet A. 2016 Feb;170A(2):322-328. doi: 10.1002/ajmg.a.37432. Epub 2015 Oct 20. Review.

PMID:
26481852
35.

Microscopic Endodontics in Infected Root Canal with Calcified Structure: A Case Report.

Suehara M, Sano Y, Sako R, Aida N, Fujii R, Muramatsu T, Furusawa M.

Bull Tokyo Dent Coll. 2015;56(3):169-75. doi: 10.2209/tdcpublication.56.169.

36.

Esophageal intramural pseudodiverticulosis of the residual esophagus after esophagectomy for esophageal cancer.

Takeshita N, Kanda N, Fukunaga T, Kimura M, Sugamoto Y, Tasaki K, Uesato M, Sazuka T, Maruyama T, Aida N, Tamachi T, Hosokawa T, Asai Y, Matsubara H.

World J Gastroenterol. 2015 Aug 14;21(30):9223-7. doi: 10.3748/wjg.v21.i30.9223.

37.

Actin stabilization induces apoptosis in cultured porcine epithelial cell rests of Malassez.

Aida N, Ushikubo T, Kobayashi F, Sako R, Suehara M, Furusawa M, Muramatsu T.

Int Endod J. 2016 Jul;49(7):663-9. doi: 10.1111/iej.12494. Epub 2015 Jul 20.

PMID:
26118334
38.

Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: A case report.

Sato T, Muroya K, Asakura Y, Yachie A, Nishimura G, Aida N, Machida J, Tanaka Y, Hasegawa T, Adachi M.

Am J Med Genet A. 2015 Oct;167A(10):2430-4. doi: 10.1002/ajmg.a.37193. Epub 2015 Jun 8.

PMID:
26059403
39.

A postzygotic NRAS mutation in a patient with Schimmelpenning syndrome.

Kuroda Y, Ohashi I, Enomoto Y, Naruto T, Baba N, Tanaka Y, Aida N, Okamoto N, Niihori T, Aoki Y, Kurosawa K.

Am J Med Genet A. 2015 Sep;167A(9):2223-5. doi: 10.1002/ajmg.a.37135. Epub 2015 Apr 25. No abstract available.

PMID:
25914220
40.

Age-related changes of susceptibility-weighted imaging in subependymal nodules of neonates and children with tuberous sclerosis complex.

Niwa T, Aida N, Fujii Y, Nozawa K, Imai Y.

Brain Dev. 2015 Nov;37(10):967-73. doi: 10.1016/j.braindev.2015.04.003. Epub 2015 Apr 20.

PMID:
25907013
41.

Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.

Asakura Y, Muroya K, Hanakawa J, Sato T, Aida N, Narumi S, Hasegawa T, Adachi M.

Clin Pediatr Endocrinol. 2015 Jan;24(1):27-32. doi: 10.1297/cpe.24.27. Epub 2015 Feb 10.

42.

Intracranial Hemorrhage and Tortuosity of Veins Detected on Susceptibility-weighted Imaging of a Child with a Type IV Collagen α1 Mutation and Schizencephaly.

Niwa T, Aida N, Osaka H, Wada T, Saitsu H, Imai Y.

Magn Reson Med Sci. 2015;14(3):223-6. doi: 10.2463/mrms.2014-0060. Epub 2014 Dec 15. Erratum in: Magn Reson Med Sci. 2015;14(4):373.

43.

Position statement from the Japan Geriatrics Society 2012: End-of-life care for the elderly.

Japanese Geriatric Society Ethics Committee, Iijima S, Aida N, Ito H, Endo H, Ohrui T, Sodei T, Toba K, Hara K, Momose Y, Uemura K, Nakano H, Miura H, Kuzuya M.

Geriatr Gerontol Int. 2014 Oct;14(4):735-9. Review. No abstract available.

PMID:
25489649
44.

Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy.

Kodera H, Osaka H, Iai M, Aida N, Yamashita A, Tsurusaki Y, Nakashima M, Miyake N, Saitsu H, Matsumoto N.

J Hum Genet. 2015 Feb;60(2):97-101. doi: 10.1038/jhg.2014.103. Epub 2014 Dec 4.

PMID:
25471517
45.

A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy.

Takano K, Tsuyusaki Y, Sato M, Takagi M, Anzai R, Okuda M, Iai M, Yamashita S, Okabe T, Aida N, Tsurusaki Y, Saitsu H, Matsumoto N, Osaka H.

Brain Dev. 2015 Jun;37(6):638-42. doi: 10.1016/j.braindev.2014.10.002. Epub 2014 Oct 27.

PMID:
25457085
46.

Clinical characteristics and outcomes of Möbius syndrome in a children's hospital.

Matsui K, Kataoka A, Yamamoto A, Tanoue K, Kurosawa K, Shibasaki J, Ohyama M, Aida N.

Pediatr Neurol. 2014 Dec;51(6):781-9. doi: 10.1016/j.pediatrneurol.2014.08.011. Epub 2014 Aug 27.

PMID:
25306435
47.

Treatment outcomes and late toxicities in patients with embryonal central nervous system tumors.

Odagiri K, Omura M, Hata M, Aida N, Niwa T, Goto H, Ito S, Adachi M, Yoshida H, Yuki H, Inoue T.

Radiat Oncol. 2014 Sep 11;9:201. doi: 10.1186/1748-717X-9-201.

48.

Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing loss.

Nakashima M, Takano K, Osaka H, Aida N, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N.

J Hum Genet. 2014 Aug;59(8):471-4. doi: 10.1038/jhg.2014.51. Epub 2014 Jun 26.

PMID:
24965255
49.

An endodontic-periodontal lesion with primary periodontal disease: a case report on its bacterial profile.

Fujii R, Muramatsu T, Yamaguchi Y, Asai T, Aida N, Suehara M, Morinaga K, Furusawa M.

Bull Tokyo Dent Coll. 2014;55(1):33-7.

50.

A rapid screening with direct sequencing from blood samples for the diagnosis of Leigh syndrome.

Shimbo H, Takagi M, Okuda M, Tsuyusaki Y, Takano K, Iai M, Yamashita S, Murayama K, Ohtake A, Goto YI, Aida N, Osaka H.

Mol Genet Metab Rep. 2014 Apr 1;1:133-138. eCollection 2014.

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